HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl N-(2-hydroxy-4-nitrophenyl)carbamate → 5-Amino-2-(benzyloxycarbonylamino)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl N-(2-hydroxy-4-nitrophenyl)carbamate | HCID 14745732 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-2-(benzyloxycarbonylamino)phenol | HCID 14745733 | — |
Reaction Steps
0.53 mole (153 g) of 2-(benzyloxycarbonylamino) -5-nitrophenol in 1 liter of ethanol is subjected to a hydrogen pressure of 8×105 pascals (8 bars) in an autoclave in the presence of 60 g of Raney nickel (water content 50%). After 1 hour at 65° C., the reaction medium is filtered while hot in order to remove the catalyst. On cooling the filtrate, the expected product crystallizes. After draining and drying, the product obtained is recrystallized in 96° strength ethanol. It melts at 148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05145483 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-f470ef3bc6324a3f891ce7bc2cfc7601 |
| Source note | uspto-grants-1992_09 |